Found 3 hits for monomerid = 50372671 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Carbonic anhydrase 9
(Homo sapiens (Human)) | BDBM50372671
(CHEMBL270994)Show SMILES CC(=O)N[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H]1n1cc(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C22H27N5O10S/c1-11(28)24-19-21(36-14(4)31)20(35-13(3)30)18(10-34-12(2)29)37-22(19)27-9-17(25-26-27)15-5-7-16(8-6-15)38(23,32)33/h5-9,18-22H,10H2,1-4H3,(H,24,28)(H2,23,32,33)/t18-,19-,20-,21-,22-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 101 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Griffith University
Curated by ChEMBL
| Assay Description Inhibition of human CA9 catalytic domain by CO2 hydration method |
J Med Chem 51: 1945-53 (2008)
Article DOI: 10.1021/jm701426t BindingDB Entry DOI: 10.7270/Q28P61CM |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM50372671
(CHEMBL270994)Show SMILES CC(=O)N[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H]1n1cc(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C22H27N5O10S/c1-11(28)24-19-21(36-14(4)31)20(35-13(3)30)18(10-34-12(2)29)37-22(19)27-9-17(25-26-27)15-5-7-16(8-6-15)38(23,32)33/h5-9,18-22H,10H2,1-4H3,(H,24,28)(H2,23,32,33)/t18-,19-,20-,21-,22-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 440 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Griffith University
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA2 by CO2 hydration method |
J Med Chem 51: 1945-53 (2008)
Article DOI: 10.1021/jm701426t BindingDB Entry DOI: 10.7270/Q28P61CM |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 1
(Homo sapiens (Human)) | BDBM50372671
(CHEMBL270994)Show SMILES CC(=O)N[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H]1n1cc(nn1)-c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C22H27N5O10S/c1-11(28)24-19-21(36-14(4)31)20(35-13(3)30)18(10-34-12(2)29)37-22(19)27-9-17(25-26-27)15-5-7-16(8-6-15)38(23,32)33/h5-9,18-22H,10H2,1-4H3,(H,24,28)(H2,23,32,33)/t18-,19-,20-,21-,22-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Griffith University
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA1 by CO2 hydration method |
J Med Chem 51: 1945-53 (2008)
Article DOI: 10.1021/jm701426t BindingDB Entry DOI: 10.7270/Q28P61CM |
More data for this Ligand-Target Pair | |